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Updated: Jun 24, 2026

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
CNVs and genetic medicine (excitement and consequences of a rediscovery)
J S Beckmann1, A J Sharp, S E Antonarakis
1Service and Department of Medical Genetics, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne (Switzerland).
Abstract:
The extensive variability of individual human genomes contributes to phenotypic variability. Structural genomic variants, and copy number variants (CNVs) in particular, have recently been rediscovered as contributors to the genomic plasticity and evolution and as pathoetiologic elements for both monogenic and complex traits. Herein we review some of the consequences of CNVs in the context of human inherited diseases.
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