Chromosomal Microarray Analysis (CMA)
Designed for prenatal diagnostic scenarios, this package supports copy number variation detection, result interpretation, and standardized clinical reporting.
Package Contents
- Fetal sample CNV detection
- Microdeletion and microduplication screening
- Clinical interpretation support
- Standardized reporting delivery
Suitable For
Applicable to advanced maternal age, high-risk prenatal screening, abnormal ultrasound findings, adverse pregnancy history, and further prenatal genetic evaluation needs.
Project Notes
CMA can identify submicroscopic copy number changes beyond conventional karyotyping and is widely used as an important tool in prenatal diagnosis.