Common aneuploidies
Trisomies 13, 18, 21 plus rare trisomies 9 and 16
Prequel NIPT Karyo Advance
Most complete non-invasive chromosomal screening available
Comprehensive Chromosomal Analysis
Combines the genome-wide CNV detection of Karyo testing with the targeted microdeletion panel, providing the most complete chromosomal screening available non-invasively.
Clinical Utility:
Sex chromosome conditions
All aneuploidies (Turner, Klinefelter, XXX, XYY, etc.)
Large CNVs (>7Mb)
Genome-wide deletions/duplications affecting multiple genes
Microdeletions (<1Mb)
23 clinically significant small deletions including DiGeorge, Prader-Willi, Angelman, Cri-du-chat, and 19 others
Associated Conditions:
This comprehensive panel detects hundreds of potential chromosomal abnormalities ranging from common, well-characterized syndromes to rare CNVs with variable presentations. See previous test descriptions for specific conditions.
Ideal for:
High-risk pregnancies, abnormal ultrasound findings, advanced maternal age, family history of chromosomal disorders, or patients desiring maximum non-invasive screening coverage.
