Microarray 60K AFCVSCB: Advanced Prenatal Genetic Testing
Comprehensive Introduction to Chromosomal Microarray Analysis
The Microarray 60K AFCVSCB represents a revolutionary advancement in prenatal genetic diagnostics, offering unprecedented resolution in detecting chromosomal abnormalities. This cutting-edge test utilizes Agilent’s microarray technology platform to analyze 60,000 genetic markers simultaneously, providing a comprehensive view of the fetal genome. Unlike traditional karyotyping methods, this sophisticated approach can identify submicroscopic chromosomal changes that may be associated with developmental disorders, intellectual disabilities, and congenital anomalies.
What Makes This Test Essential for Modern Prenatal Care?
Chromosomal microarray analysis has become the gold standard in prenatal genetic testing due to its superior detection capabilities. The 60K resolution ensures that even the smallest genetic variations are identified, offering expectant parents and healthcare providers crucial information for making informed decisions about pregnancy management and future care planning.
What the Microarray 60K AFCVSCB Detects
This comprehensive genetic screening test identifies a wide range of chromosomal abnormalities with exceptional precision:
- Copy number variations (CNVs) including microdeletions and microduplications
- Chromosomal imbalances undetectable by conventional methods
- Subtelomeric rearrangements and interstitial deletions
- Uniparental disomy in specific chromosomal regions
- Mosaicism at levels as low as 10-20%
Advanced Detection Capabilities
The test’s 60,000-probe design provides resolution approximately 100 times greater than traditional G-banded chromosome analysis, enabling detection of abnormalities as small as 50-100 kilobases in size. This level of detail is particularly valuable for identifying genetic conditions associated with developmental delays, autism spectrum disorders, and multiple congenital anomalies.
Who Should Consider Microarray 60K AFCVSCB Testing?
This advanced prenatal genetic test is recommended for various clinical scenarios:
- Pregnancies with abnormal ultrasound findings including structural anomalies
- Cases with increased nuchal translucency or other soft markers
- Women of advanced maternal age (35 years or older)
- Previous pregnancy with chromosomal abnormalities
- Family history of genetic disorders or developmental delays
- Unexplained fetal growth restriction
- Parental balanced chromosomal rearrangements
Clinical Indications and Risk Factors
Healthcare providers often recommend this test when traditional screening methods indicate elevated risk or when there are specific concerns about fetal development. The test provides valuable information regardless of whether ultrasound findings are present, making it an essential tool for comprehensive prenatal assessment.
Significant Benefits of Microarray 60K Testing
Choosing this advanced genetic analysis offers numerous advantages for expectant parents and healthcare providers:
- Enhanced Detection Rates: Identifies 15-20% more clinically significant abnormalities compared to standard karyotyping
- Early Intervention Planning: Provides critical information for preparing medical care and support services
- Comprehensive Risk Assessment: Offers a complete picture of genetic health beyond what routine screening can provide
- Peace of Mind: Reduces uncertainty and anxiety through detailed genetic information
- Informed Decision Making: Empowers families with knowledge for pregnancy management decisions
Clinical Utility and Patient Outcomes
The information obtained from microarray testing can significantly impact pregnancy management, delivery planning, and neonatal care preparation. Early identification of genetic conditions allows for appropriate medical consultations, specialized care coordination, and family support services.
Understanding Your Test Results
Interpreting microarray results requires specialized expertise, and our genetic counselors provide comprehensive explanations:
- Normal Results: No clinically significant chromosomal abnormalities detected
- Pathogenic Findings: Identified genetic variations known to cause medical conditions
- Variants of Uncertain Significance (VUS): Genetic changes with unknown clinical implications requiring further evaluation
- Benign Variations: Common genetic differences not associated with health concerns
Post-Test Guidance and Support
Our team provides detailed counseling to help you understand your results and their implications. We discuss potential next steps, available resources, and connect you with appropriate specialists when needed. All results are reviewed by board-certified geneticists to ensure accurate interpretation and clinical relevance.
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $488 |
| Regular Price | $650 |
Sample Requirements and Processing
The test requires samples collected in sterile containers with normal saline. Acceptable sample types include amniotic fluid, chorionic villi, or cord blood. Turnaround time is typically 7-9 days from sample receipt at our laboratory.
Nationwide Availability and Booking Information
We have diagnostic centers conveniently located across major US cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality testing standards nationwide.
Simple Booking Process
Schedule your Microarray 60K AFCVSCB test today by calling our dedicated genetics hotline at +1(267) 388-9828 or visiting your nearest GGC DNA center. Our genetic counselors are available to answer questions and guide you through the testing process.
Why Choose GGC DNA for Your Prenatal Genetic Testing?
As a leader in genetic diagnostics, we combine cutting-edge technology with compassionate care. Our certified laboratory professionals, board-certified geneticists, and experienced counselors work together to provide accurate results and comprehensive support throughout your testing journey.
Take the next step in comprehensive prenatal care. Contact us today to schedule your Microarray 60K AFCVSCB test and gain valuable insights into your baby’s genetic health.
