Large Copy-Number Variants in UK Biobank Caused by Clonal Hematopoiesis May Confound Penetrance Estimates
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference37 articles.
1. A copy number variation map of the human genome;Zarrei;Nat. Rev. Genet.,2015
2. Origins and functional impact of copy number variation in the human genome;Conrad;Nature,2010
3. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls;Craddock;Nature,2010
4. A structural variation reference for medical and population genetics;Collins;Nature,2020
5. A copy number variation morbidity map of developmental delay;Cooper;Nat. Genet.,2011
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