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Description
PrenatalSafe Karyo Complete Plus represent the most comprehensive information available from a non invasive prenatal test to date. PrenatalSafe Karyo Complete Plus analyzes both numerical (aneuploidies) and structural (deletion/duplication) anomalies on all the chromosomes and 9 among the most common microdelection syndromes. PrenatalSafe Complete also screens for several life-altering genetic disorders that are not screened with current NIPT technology. Not suitable for dichorionic twin pregnancy.
External Information
Click here for more information about the PrenatalSafe Complete® Plus genetic test.Additional information
Samples | Streck |
---|---|
Method of testing | NGS |
Turnaround Time (TAT) | 5-10 days |
Number of Genes | 29 |
Genes / Chromosomes / SNPs | all chromosomes + 9 microdeletions + 28 genes: ASXL1, BRAF, CBL, CFTR, CHD7, COL1A1, COL1A2, COL2A1, FGFR2, FGFR3, GJB2, GJB6, HBB, HDAC8, JAG1, KRAS, MAP2K1, MAP2K2, MECP2, NIPBL, NRAS, NSD1, PTPN11, RAF1, RIT1, SETBP1, SHOC2, SIX3, SOS1 |
External Information | Click here for more information about the PrenatalSafe Complete® Plus genetic test. |