Microarray 180K (AF/CVS/CB/POC/PB) Test
Short Name: Microarray 180K
Also known as: Chromosomal Microarray Analysis, CMA 180K
Microarray 180K (AF/CVS/CB/POC/PB) Test test available at DNA Labs India for ₹28,500. Uses Microarray Analysis, Agilent Technology on Amniotic fluid, Chorionic villi, Products of Conception, Cord blood, Peripheral blood samples. Results in 7-9 days. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The purpose of the Microarray 180K test is to identify chromosomal abnormalities and genetic variations that may cause various health conditions. It aids in the diagnosis of genetic disorders, guides treatment decisions, and provides information for genetic counseling.
- Test Code
- 3084
- Price
- ₹28,500
- Sample Type
- Amniotic fluid, Chorionic villi, Products of Conception, Cord blood, Peripheral blood
- Result Time
- 7-9 days
- Fasting Required
- No
- Method
- Microarray Analysis, Agilent Technology
Sample Collection
Consult with a physician for prescription if required. For prenatal samples, specific procedures like amniocentesis or CVS may be needed.
Method: Blood draw or amniocentesis/CVS depending on sample type
Laboratory Analysis
Sample collection is performed by a trained professional. For blood samples, a standard blood draw is done. For amniotic fluid or CVS, specialized procedures are used.
Report Delivery
Sample is sent to the lab for analysis. Results are communicated to the physician.
Timeline: 7-9 days
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the Microarray 180K test is to identify chromosomal abnormalities and genetic variations that may cause various health conditions. It aids in the diagnosis of genetic disorders, guides treatment decisions, and provides information for genetic counseling.
How to Prepare
- Ensure proper labeling of samples
- Use appropriate containers as specified
- Maintain sample stability during transport
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for early diagnosis of chromosomal abnormalities in prenatal and postnatal cases, aiding in timely intervention and genetic counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed samples
- Insufficient sample volume
- Improperly labeled samples
Understanding Your Results
If results are abnormal or if there are concerns about genetic disorders, consult a geneticist or specialist for further evaluation and management.
Limitations
- ⚠May not detect all genetic variations
- ⚠Results may include variants of uncertain significance (VUS)
- ⚠Requires interpretation by a geneticist
Risks & Considerations
- ●For amniocentesis/CVS: Risk of miscarriage or infection
- ●For blood draw: Minor bruising or discomfort
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Technical errors
Compare With Similar Tests
| Test | Microarray 180K (AF/CVS/CB/POC/PB) | Karyotyping | Fluorescence In Situ Hybridization (FISH) | Whole Exome Sequencing |
|---|---|---|---|---|
| Comparison | Microarray 180K (AF/CVS/CB/POC/PB) | Microarray detects smaller variations than karyotyping | Microarray is more comprehensive than FISH for multiple loci | Microarray focuses on copy number variations, while WES detects point mutations |
Frequently Asked Questions
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Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
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