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. 2019 Oct 15;12(10):e002694. doi: 10.1161/CIRCGEN.119.002694

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© 2019 The Authors.

Circulation: Genomic and Precision Medicine is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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Figure 2. — Intersection of copy number variant (CNV) and whole-exome sequencing (WES) data. Numbers of genes involved in the final stages of the workflow depicted in Figure 1 are shown. Genes with assigned phenotypes (circles with dashed line) were excluded from further analysis. BOTH indicates deleted/duplicated; DEL, deletion; DUP, duplication; OMIM, Online Mendelian Inheritance in Man; and TOF, Tetralogy of Fallot.