Effective July 31, 2018, CooperGenomics will no longer be accepting samples for carrier screening and noninvasive prenatal testing (NIPT). We remain committed to serving as your trusted partner in preimplantation genetic testing. Click here for more details.

DISEASE LIST

ChromoMap NIPS screens for aneuploidies and microdeletions that can significantly impact a child’s health and quality of life or cause adverse pregnancy outcomes.


Standard Panel

The standard panel screens for three trisomies. A trisomy is an extra copy of an entire chromosome.

  • Trisomy 21 (Down Syndrome)
  • Trisomy 13 (Patau Syndrome)
  • Trisomy 18 (Edwards Syndrome)

Optional Add-Ons*

Sex Chromosome Aneuploidies

Sex aneuploidies are missing or extra copies of the sex chromosomes, X and Y.

  • Monosomy X (Turner Syndrome)
  • XXX (Triple X Syndrome)
  • XXY (Klinefelter Syndrome)
  • XYY (Jacob Syndrome)

All Other Autosomal Aneuploidies

Microdeletions

A microdeletion is a change in which a small segment of genetic material is missing from a specific chromosome.

  • 22q11.2 (DiGeorge syndrome, Velocardiofacial Syndrome)
  • 1p36 Deletion Syndrome
  • 15q11.2 (Angelman/Prader Willi Syndrome)
  • 5p- (Cri du Chat Syndrome)
  • 4p- (Wolf-Hirschhorn Syndrome)

*Add-on panels available for singleton pregnancies only.

If sex aneuploidies are screened for, the fetal sex will be identified.

ChromoMap NIPS is a screening test. Diagnostic tests such as amniocentesis or CVS are available to confirm results. However, because these tests are invasive, they carry a risk of complications, including miscarriage.

Effective July 31, 2018, CooperGenomics will no longer be accepting samples for carrier screening and noninvasive prenatal testing (NIPT). We remain committed to serving as your trusted partner in preimplantation genetic testing. Click here for more details.

PANELS

Serenity NIPT screens for abnormalities that can significantly impact a child’s health and quality of life or cause adverse pregnancy outcomes.

Serenity testing is offered as four different panel options, providing options to accommodate every patient’s unique situation. Serenity Basic and Serenity 24 are available for both singleton and twin pregnancies.

Serenity Basic

Screens for the following:

checkmark Common Trisomies

  • Trisomy 21 (Down syndrome)
  • Trisomy 18 (Edwards syndrome)
  • Trisomy 13 (Patau syndrome)

checkmark Sex Aneuploidies (optional)

  • Monosomy X (Turner syndrome)
  • XXX (Triple X syndrome)
  • XXY (Klinefelter syndrome)
  • XYY (Jacob syndrome)
  • Fetal Sex Determination

 

Serenity 24

Screens for the following:

checkmark All Autosomal Aneuploidies

  • Trisomy 21 (Down syndrome)
  • Trisomy 18 (Edwards syndrome)
  • Trisomy 13 (Patau syndrome)
  • All Other Autosomal Aneuploidies

checkmark Sex Aneuploidies (optional)

  • Monosomy X (Turner syndrome)
  • XXX (Triple X syndrome)
  • XXY (Klinefelter syndrome)
  • XYY (Jacob syndrome)
  • Fetal Sex Determination

 

Serenity Plus

Screens for the following:

checkmark Common Trisomies

  • Trisomy 21 (Down syndrome)
  • Trisomy 18 (Edwards syndrome)
  • Trisomy 13 (Patau syndrome)

checkmark Microdeletions

  • 22q11.2 (DiGeorge syndrome, Velocardiofacial syndrome)
  • 1p36 Deletion syndrome
  • 15q11.2 (Angelman/Prader Willi syndrome)
  • 5p- (Cri du Chat syndrome)
  • 4p- (Wolf-Hirschhorn syndrome)

checkmark Sex Aneuploidies (optional)

  • Monosomy X (Turner syndrome)
  • XXX (Triple X syndrome)
  • XXY (Klinefelter syndrome)
  • XYY (Jacob syndrome)
  • Fetal Sex Determination

 

Serenity Comprehensive

Screens for the following:

checkmark All Autosomal Aneuploidies

  • Trisomy 21 (Down syndrome)
  • Trisomy 18 (Edwards syndrome)
  • Trisomy 13 (Patau syndrome)
  • All Other Autosomal Aneuploidies

checkmark Microdeletions

  • 22q11.2 (DiGeorge syndrome, Velocardiofacial syndrome)
  • 1p36 Deletion syndrome
  • 15q11.2 (Angelman/Prader Willi syndrome)
  • 5p- (Cri du Chat syndrome)
  • 4p- (Wolf-Hirschhorn syndrome)

checkmark Sex Aneuploidies (optional)

  • Monosomy X (Turner syndrome)
  • XXX (Triple X syndrome)
  • XXY (Klinefelter syndrome)
  • XYY (Jacob syndrome)
  • Fetal Sex Determination