Prenatal CMA reflex to ExomeDx™ Prenatal
Prenatal Whole Genome Chromosomal Microarray (Prenatal CMA) with automatic reflex to ExomeDx™ Prenatal, trio if the CMA does not sufficiently account for the fetus’s phenotype. A second report will be issued if the reflex is activated.
Test Overview
Clinical Utility
- Testing of prenatal samples, both ongoing and deceased fetuses
- Identification of underlying molecular diagnosis
- Recurrence risk assessment
Test Details
Conditions
- Fetus with ultrasound anomalies
Lab Method
- Next-Gen Sequencing
- Whole Genome Chromosomal Microarray
Ordering Information
Important Information
Prenatal Whole Genome Chromosomal Microarray (Prenatal CMA) with automatic reflex to ExomeDx™ Prenatal, trio if the CMA does not sufficiently account for the fetus’s phenotype. A second report will be issued if the reflex is activated.
Resources
Test Documents
Billing
Targeted Variant Testing