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. 2019 Jun 28;7(8):e774. doi: 10.1002/mgg3.774

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© 2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc.

This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/3.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

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Summary of CYP1B1 entire gene deletions. Schematic drawing of the 2p22.2 region showing known human protein‐coding genes from the NCBI reference sequence (RefSeq) as seen in DECIPHER (http://decipher.sanger.ac.uk) using the GRCh37/hg19 assembly. The 119kb deletion reported in this study is shown in a solid red line (chr2: 38,239,356–38,358,664). Previously reported deletions are displayed in solid green lines (146kb, chr2: 38,222,086–38,368,231 (Kelberman, 2011); 193 kb, chr2: 38,191,823–38,385,253 (Damjanovich, 2013); 162kb, chr2: 38,187,289–38,349,505 (Milla, 2013))