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. 2016 May 15;8:17. doi: 10.1186/s11689-016-9147-8

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© Gialluisi et al. 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 — Candidate region of CNV overlap associated with PC1 in the GWAS with CNV state. The red line indicates the associated interval chr15:32,380,064-32,514,341, partially overlapping CHRNA7 (15q13.3). Black horizontal lines represent the individual CNV calls detected in this region (nine heterozygous duplications and one heterozygous deletion; see Additional file 2: Table S2e for details)