Nateraa
|
Panorama |
21, 18, 13 |
45,X (Turner syndrome), 47,XXY (Klinefelter syndrome), 47,XXX (Triple X syndrome), 47,XYY (XYY syndrome) |
22q11.2 (DiGeorge syndrome), 1p36 deletion, 5p (Cri-du chat syndrome), 15q11.2 (Angelman and Prader-Willi syndrome) |
SNP analysis via sequencing |
High Risk, Low Risk |
Illuminab
|
Verifi |
21, 18, 16, 13, 9 |
45,X (Turner syndrome), 47,XXY (Klinefelter syndrome), 47,XXX (Triple X syndrome), 47,XYY (XYY syndrome) |
22q11.2 (DiGeorge syndrome), 1p36, 15q11.2 (Angelman, Prader-Willi syndromes) 5p (Cri-du-chat syndrome), and 4p (Wolf-Hirschhorn syndrome) |
Genome-wide sequencing |
No Aneuploidy Detected, Aneuploidy Detected, or Aneuploidy Suspected (Borderline Value) |
Sequenomc
|
MaterniT21 Plus |
22, 21, 18, 16, 13 |
45,X (Turner syndrome), 47,XXY (Klinefelter syndrome), 47,XXX (Triple X syndrome), 47,XYY (XYY syndrome) |
22q11.2 (DiGeorge syndrome), 1p36 deletion, 5p (Cri-du-chat syndrome), 15q11.2 (Angelman and Prader-Willi syndrome) 4p (Wolf-Hirschhorn syndrome), 8q (Langier-Gideon syndrome), 11q (Jacobsen syndrome) |
Genome-wide sequencing |
Positive, Negative, Additional Finding |
Ariosad
|
Harmony |
21, 18, 13 |
Yes |
No |
Targeted sequencing/array |
High Risk, Low Risk |