Abstract

Given the similar resolution for subchromosomal anomalies between karyotype (5-10Mb) and genome-wide non-invasive prenatal screening (gwNIPS) (7Mb), extrapolation of gwNIPS performance using a historical cohort is reasonable. Our objective is to estimate the post-test probabilities of gwNIPS for advanced maternal age (AMA) only vs. sonographic structural abnormalities (SA) using a historical cohort of invasive diagnostic testing.

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