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. Author manuscript; available in PMC: 2017 May 11.
Published in final edited form as: Genet Med. 2016 Sep 22;19(5):559–567. doi: 10.1038/gim.2016.145

Table 4.

Technology Platforms and Test Offerings of Four Major NIPS Test Companies

Company Test Name Trisomies Sex Chromosome Aneuploidy Microdeletions Technology Platform Results Reported
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