Karyotyping
See the Bigger Picture—With Every Chromosome Counted

Karyotyping
Karyotyping provides a visual map of your chromosomes to detect large-scale abnormalities like aneuploidies, translocations, and inversions. Whether for infertility investigations, prenatal evaluations, or suspected chromosomal disorders, this test offers foundational genetic insights that support informed decision-making and diagnosis.

What Does It Do?
Karyotyping provides a visual assessment of the number and structure of chromosomes. It detects large-scale abnormalities like translocations, inversions, and aneuploidies.
Polygenic Risk Score (PRS)
Not applicable; no PRS used. Interpretation is based on visible chromosomal changes.
Who Benefits?
Couples experiencing infertility or recurrent miscarriages.
Individuals with suspected chromosomal disorders.
Prenatal evaluations and birth defect investigations.
Core Pillars
Count and Compare
Analyze chromosome count and structure.
Confirm Syndromes
Validate suspected chromosomal syndromes.
Counsel with Clarity
Genetic counselling based on results.
MyDNA Gene Proactive
Fostering well-being by assessing and managing predisposition of traits, lifestyle diseases and chronic health conditions.
Free Consultation
Speak with our genetic counselors
Technical Specifications
Specification | Value |
---|---|
Technique | G-banding |
Platform | Microscopy-based cytogenetics |
Resolution | 5–10 Mb |
Sample Type | Blood (lymphocyte culture) |
Turnaround Time | 10–14 days |
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