This test is not orderable.

MaterniT21 Plus CORE + Microdeletions and Sex Chromosome Aneuploidy Build info

Synonyms

  • MATERNIT21 PLUS CORE + MICRODELETIONS AND FETAL GENDER
  • MATERNITMD
  • NIPT
  • NIPS
  • LAB4155

Short Name

MATERNIT21 PLUS CORE + MICRODELETIONS AND FETAL GENDER

Procedure Master Number

LAB4155

Procedure ID

189707

Clinical Info

For pregnancies at increased risk of fetal abnormalities, the MaterniT21 PLUS test delivers a comprehensive NIPT for the analysis of chromosomal regions including trisomies 21, 18, and 13, fetal sex, sex chromosome aneuploidies, and an enhanced sequencing series that examines seven clinically relevant microdeletions and two additional chromosomal regions, trisomies 22 and 16.

Specimen Sources

Blood, Arterial Blood, Capillary Blood, Central Line Blood, Venous

Specimen Types

Blood

Container

Streck Tube

Collection Instructions

Container/Tube:  Streck Tube 
Specimen:  10 ml Whole Blood ( 8 mL min)
Special Instructions   The following information must be provided with the test request form: patient's date of birth, gestational age, additional patient demographic information, pregnancy type (singleton or multiple), donor egg status and the clinical indications (including advanced maternal age, abnormal ultrasound, history suggestive of increased risk for aneuploidy, positive serum screen, or other indications).

Transport Instructions

Room Temperature

Specimen Stability

7 Days Room Temperature

Methodology

Cell-Free DNA

Days Performed

TAT  4-6 days

Performing Laboratory

LabCorp- Sequenom

CPT

81420
81422

PDM

245461

Only Orderable at Locations:

Orderable Everywhere

Results

Component Name Base Name Common Name External Name
E DUE DATE EDUEDT E DUE DATE E Due Date
GESTATION GESTATION GESTATION Gestation
FETAL FRACTION FETALFRACT FETAL FRACTION
GESTATIONAL AGE > OR = 9W: GESTAGE GESTATIONAL AGE GREATER THAN OR EQUAL TO 9W Gestational Age > Or = 9W:
TEST RESULT TESTRESULT TEST RESULT Test Result
LAB DIRECTOR COMMENTS LABDIRCOM LAB DIRECTOR COMMENTS Lab Director Comments
APPROVED BY APPORVEDBY APPROVED BY Approved By
TRISOMY 21 (DOWN SYND) TRISOMY21 TRISOMY 21 (DOWN SYND) TRISOMY 21 (DOWN SYND)
TRISOMY 18 (EDWARDS SYND) TRISOMY18 TRISOMY 18 (EDWARDS SYND) TRISOMY 18 (EDWARDS SYND)
TRISOMY 13 (PATAU SYND) TRISOMY13 TRISOMY 13 (PATAU SYND) TRISOMY 13 (PATAU SYND)
FETAL SEX FETALSEX FETAL SEX Fetal Sex
MONOSOMY X (TURNER SYNDROME) MONOSOMYX MONOSOMY X TURNER SYNDROME Monosomy X (Turner Syndrome)
XYY (JACOBS SYNDROME) XYY XYY JACOBS SYNDROME Xyy (Jacobs Syndrome)
XXY (KLINEFELTER SYNDROME) XXY XXY KLINEFELTER SYNDROME Xxy (Klinefelter Syndrome)
XXX (TRIPLE X SYNDROME) XXX XXX TRIPLE X SYNDROME Xxx (Triple X Syndrome)
22Q11 DELETION (DIGEORGE) 22Q11DELET 22Q11 DELETION DIGEORGE 22Q11 Deletion (Digeorge)
15Q11 DELETION (PW ANGELMAN) 15Q11DELET 15Q11 DELETION PW ANGELMAN 15Q11 Deletion (Pw Angelman)
11Q23 DELETION (JACOBSEN) 11Q23DELET 11Q23 DELETION JACOBSEN 11Q23 Deletion (Jacobsen)
8Q24 DELETION (LANGER-GIEDION) 8Q24DELET 8Q24 DELETION LANGER GIEDION 8Q24 Deletion (Langer-Giedion)
5P15 DELETION (CRI-DU-CHAT) 5P15DELET 5P15 DELETION CRI DU CHAT 5P15 Deletion (Cri-Du-Chat)
4P16 DELETION(WOLF-HIRSCHHORN) 4P16DELET 4P16 DELETION WOLF HIRSCHHORN 4P16 Deletion(Wolf-Hirschhorn)
1P36 DELETION SYNDROME RESULT 1P36DELSYN 1P36DELSYN
TRISOMY 16 TRIS16 TRISOMY 16
TRISOMY 22 TRIS22 TRISOMY 22
NEGATIVE PREDICTIVE VALUE NEGPREDVAL NEGATIVE PREDICTIVE VALUE
POSITIVE PREDICTIVE VALUE POSPREDVAL POSITIVE PREDICTIVE VALUE Positive Predictive Value
ABOUT THE TEST ABOUTTEST ABOUT THE TEST About The Test
TEST METHOD TESTMETH TEST METHOD Test Method
PERFORMANCE PERFORMANCE PERFORMANCE Performance
PERFORMANCE CHARACTERISTICS PERFOMCHAR PERFORMANCE CHARACTERISTICS Performance Characteristics
LIMITATIONS OF THE TEST LIMITOFTEST LIMITATIONS OF THE TEST LIMITATIONS OF THE TEST
NOTE NOTE NOTE NOTE
REFERENCES REFERENCES REFERENCES References
PDF AFP RESULT PDF PDF, RESULT Pdf Afp Result