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Article

Detection of copy number variants with chromosomal microarray in 10 377 pregnancies at a single laboratory.

Acta obstetricia et gynecologica Scandinavica - 1 Jun 2020

Lin Yi-Hui, Jong Yiin-Jeng, Huang Pin-Chia, Tsai Chris

Abstract excerpt

INTRODUCTION: Invasive prenatal testing with chromosomal microarray analysis may be a relevant option for all pregnant women, but there is only moderate-quality evidence for such an offer. We intended to study the prevalence of copy number variants (CNVs) in prenatal samples using a single SNP-array platform stratified by indication. MATERIAL AND METHODS: A cross-sectional study was performed based on a cohort....

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 32346853
DOI: 10.1111/aogs.13886
PMCID: PMC7383919

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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