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26069 MaterniT Genome

MaterniT Genome
Test Code: MATGNSO
Test Components
Trisomy 21, Trisomy 18, Trisomy 13, Other autosomal aneuploidies, sex chromosome aneuploidies and fetal sex classification.  22q11 deletion, 15q11 deletion, 11q23 deletion, 8q24 deletion, 5p15 deletion, 4p16 deletion, 1p36 deletion syndrome. 
Useful For

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.

Specimen Requirements
Fasting Required Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​No ​Whole Blood ​Special Collection Tubes included in MarterniT Genome Kit ​10 mL
Collection Processing Instructions

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.

Specimen Stability Information
Specimen Type Temperature Time
​Whole Blood ​Ambient ​7 days
Rejection Criteria
Refrigerated or frozen samples are not acceptable
Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
​Sequenom Center for Molecular Medicine ​Monday through Friday ​3-5 days ​DNA Extraction
Test Information
This test was developed and its performance characteristics determined by Sequenom Center for Molecular Medicine.​
Reference Range Information
See Report
Classification
This test was developed and its performance characteristics determined by Sequenom Center for Molecular Medicine.
Test Components
Trisomy 21, Trisomy 18, Trisomy 13, Other autosomal aneuploidies, sex chromosome aneuploidies and fetal sex classification.  22q11 deletion, 15q11 deletion, 11q23 deletion, 8q24 deletion, 5p15 deletion, 4p16 deletion, 1p36 deletion syndrome. 
Ordering Applications
Ordering Application Description
​Centricity ​MaterniT Genome
​Cerner ​MaterniT Genome
​COM ​MaterniT Genome
If the ordering application you are looking for is not listed, contact your local laboratory for assistance.
Specimen Requirements
Fasting Required Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​No ​Whole Blood ​Special Collection Tubes included in MarterniT Genome Kit ​10 mL
Collection Processing

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.

Specimen Stability Information
Specimen Type Temperature Time
​Whole Blood ​Ambient ​7 days
Rejection Criteria
Refrigerated or frozen samples are not acceptable
Useful For

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.

Test Components
Trisomy 21, Trisomy 18, Trisomy 13, Other autosomal aneuploidies, sex chromosome aneuploidies and fetal sex classification.  22q11 deletion, 15q11 deletion, 11q23 deletion, 8q24 deletion, 5p15 deletion, 4p16 deletion, 1p36 deletion syndrome. 
Reference Range Information
See Report
For more information visit:
Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
​Sequenom Center for Molecular Medicine ​Monday through Friday ​3-5 days ​DNA Extraction
For billing questions, see Contacts
Classification
This test was developed and its performance characteristics determined by Sequenom Center for Molecular Medicine.
For most current information refer to the Marshfield Laboratory online reference manual.