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. 2019 Mar 4;10:1025. doi: 10.1038/s41467-019-08992-7

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — Analysis of copy number variant (CNV) in pepsinogen A cluster at chromosome 11q12.2 using multiple alignment. a Visualization of CNV haplotypes using multiple alignment of contigs allows easy counting of the repeating units. Copy numbers (CNs) are shown on the left. Alignment of all individuals across the 26 populations is provided in Supplementary Fig. 13. b A boxplot for CN in different ethnic groups. East Asians (EAS) have significantly more copies than other populations (p < 0.05, Tukey test), while Europeans (EUR) have significantly fewer copies than other populations (p < 0.05, Tukey test) except Americans (AMR)