Microarray 60K (POC) + Couple Karyotyping Test
Short Name: Microarray 60K + Karyotyping
Also known as: Chromosomal Microarray Analysis, Couple Chromosome Analysis
Microarray 60K (POC) + Couple Karyotyping Test test available at DNA Labs India for ₹18,000. Uses Microarray Analysis, Cell Culture Karyotyping on Products of Conception, Peripheral blood of parents 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
To diagnose genetic disorders, identify chromosomal abnormalities in couples, and assess causes of infertility or recurrent miscarriages through combined microarray and karyotyping analysis.
- Test Code
- 3095
- Price
- ₹18,000
- Sample Type
- Products of Conception, Peripheral blood of parents
- Result Time
- 7-9 days
- Fasting Required
- No
- Method
- Microarray Analysis, Cell Culture Karyotyping
Sample Collection
Ensure a doctor's prescription is available. Avoid eating or drinking for a few hours if specified, though fasting is not typically required.
Method: Blood draw and POC collection
Laboratory Analysis
Blood samples will be drawn from both parents using a heparinized vacutainer. POC sample will be collected in a sterile container with normal saline.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Store samples as instructed and transport to the lab promptly.
Timeline: 7-9 days
Patient Instructions
About This Test
Who Should Get This Test
To diagnose genetic disorders, identify chromosomal abnormalities in couples, and assess causes of infertility or recurrent miscarriages through combined microarray and karyotyping analysis.
How to Prepare
- Use sterile container or sterile normal saline container for POC
- Use heparinised vacutainer for parents' blood (3 ml each)
- Label samples correctly with patient details
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for couples with recurrent miscarriages or infertility to identify chromosomal abnormalities and guide treatment options."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Improper container or labeling
- Insufficient sample volume
Understanding Your Results
Normal karyotype and no CNVs detected
No chromosomal abnormalities found; genetic factors may not be the cause of issues.
Abnormal karyotype or CNVs detected
Specific chromosomal or genetic abnormalities identified; may indicate syndromes like Down syndrome or translocations.
SNPs associated with disorders
Genetic variants linked to conditions such as cystic fibrosis; further counseling recommended.
Consult a doctor if results are abnormal, if you have a family history of genetic disorders, or if planning pregnancy after receiving results.
Limitations
- ⚠May not detect all genetic variants
- ⚠Requires expert interpretation
- ⚠Cannot identify single gene disorders without additional testing
Risks & Considerations
- ●Minor bruising or pain at blood draw site
- ●Rare risk of infection
- ●Emotional stress from results
Interfering Factors
- ●Contaminated sample
- ●Insufficient sample volume
- ●Improper storage conditions
Frequently Asked Questions
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₹5,250Reference 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.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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