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. 2014 May 14;9(5):e96471. doi: 10.1371/journal.pone.0096471

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© 2014 Xie et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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(A) SNP based array shows a 1.05 Mb deletion at 17p13.2 (chr17:4041358-5091377) (Human GRCh37/hg19 Assembly). B allele frequency and Log R ratio are showed in the upper panel; (B) The lower panel shows genes mapped to the deleted region. OMIM genes are highlighted in green, DGV structure variants and Segmental Duplications are also enclosed in the lower panel.