As early as ten weeks gestation, this test can identify common whole chromosome abnormalities, as well as, extra or missing parts of chromosomes that can cause genetic conditions difficult to diagnose at birth.
Detects up to 25% more clinically relevant chromosomal information than other leading NIPTs. Provides karyotype-level insight, information about deletions or duplications of chromosome material 7 Mb or larger, as well as analysis of seven clinically relevant microdeletion regions less than 7 Mb in size.
Contact Lab Specimen Processing at 715-221-6220 or 800-222-5835 to obtain special collection kit and consent form. Form must be signed by both the patient and the clinician. The sample must be room temp, ship overnight for Mon.-Fri. delivery. If drawn at a Regional Center on a Friday, the sample would have to be sent directly from the Center to Sequenom.
Patient/Provider signature is required. If this is not obtained prior to sample collection, the sample will be sent out, but results will not be available until the required signatures are obtained.
THIS IS NOT AVAILABLE TO OUTREACH CLIENTS. Outreach clients must work directly with Sequenom Lab.