Open access
Sep 2026
Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women
Abstract Objectives Knowledge of copy number variants (CNVs) is relevant to maternal and fetal health and can be obtained from noninvasive prenatal screening (NIPS) of pregnancy. However, genome-wide analysis of maternal CNVs using NIPS data has not been conducted in large populations. Methods For CNV analysis, the hum...
Liang Hu, Xian-Zhen Cao, Shu-Xian Zeng et al.
· Annals medicus · 0 citations