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. 2016 Sep 22;9:71. doi: 10.1186/s13039-016-0282-4

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© The Author(s). 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 2 — Human Omni1-Quad SNP-array result of the 19p13.2-p13.13 in Patient 1 with Malan syndrome. SNP-based array shows a de novo 1.4 Mb deletion (chr19: 12,157,839-13,518,462/hg19). Log R ratio and B allele frequencies are showed in upper panel; the lower panel shows genes in the deleted region