Microarray 315K Single Karyotyping AFCVSCBPOCPB
Comprehensive Genetic Analysis for Chromosomal Abnormalities
The Microarray 315K Single Karyotyping test represents a cutting-edge advancement in genetic diagnostics, combining the precision of microarray technology with the comprehensive analysis of traditional karyotyping. This sophisticated testing methodology provides unparalleled insights into chromosomal structure and genetic variations that may impact health outcomes.
What This Advanced Genetic Test Measures
Our Microarray 315K Single Karyotyping test performs comprehensive analysis of:
- Chromosomal abnormalities including aneuploidies (extra or missing chromosomes)
- Microdeletions and microduplications as small as 50-100 kilobases
- Structural chromosomal rearrangements
- Copy number variations (CNVs) across the entire genome
- Over 315,000 genetic markers for comprehensive coverage
- Balanced and unbalanced chromosomal rearrangements
Who Should Consider This Genetic Testing
This comprehensive genetic analysis is recommended for individuals experiencing:
- Abnormal prenatal ultrasound findings
- Family history of chromosomal disorders
- Unexplained developmental delays or intellectual disabilities
- Multiple congenital anomalies
- Recurrent pregnancy losses
- Suspected genetic syndromes
- Advanced maternal age pregnancy concerns
- Previous abnormal prenatal screening results
Significant Benefits of Microarray Karyotyping
Choosing our advanced genetic testing provides numerous advantages:
- Higher Resolution Detection: Identifies genetic variations 100 times smaller than traditional karyotyping
- Comprehensive Analysis: Simultaneously evaluates entire genome for multiple abnormality types
- Enhanced Diagnostic Yield: Detects clinically significant findings in cases with normal karyotype results
- Personalized Risk Assessment: Provides detailed information for genetic counseling and family planning
- Clinical Decision Support: Informs medical management and treatment strategies
- Future Health Planning: Enables proactive healthcare decisions based on genetic profile
Understanding Your Test Results
Your comprehensive genetic report will include detailed interpretation of findings:
- Normal Results: No clinically significant chromosomal abnormalities detected
- Pathogenic Findings: Identification of genetic variations associated with known medical conditions
- Variants of Uncertain Significance: Genetic changes requiring further clinical correlation
- Benign Variations: Common genetic polymorphisms with no clinical significance
- Carrier Status Information: Identification of recessive genetic conditions
All results are reviewed by board-certified genetic specialists who provide clear explanations and recommendations for next steps. Genetic counseling is available to help you understand the implications of your results.
Test Pricing Information
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $450 |
| Regular Price | $600 |
Nationwide Testing Availability
We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, Austin, Jacksonville, Fort Worth, Columbus, Charlotte, San Francisco, Indianapolis, Seattle, Denver, Washington DC, Boston, El Paso, Nashville, Detroit, Oklahoma City, Portland, Las Vegas, Memphis, Louisville, Baltimore, and Milwaukee.
Take Control of Your Genetic Health Today
Don’t wait to get the comprehensive genetic insights you need for informed healthcare decisions. Our advanced Microarray 315K Single Karyotyping test provides the detailed chromosomal analysis required for accurate diagnosis and personalized medical management.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or book your test online. Our genetic specialists are ready to answer your questions and guide you through the testing process.
With a rapid 7-9 day turnaround time and sample collection from amniotic fluid, chorionic villi, products of conception, cord blood, or peripheral blood, we make comprehensive genetic testing accessible and convenient for patients nationwide.

