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. 2015 Feb 6;15:35. doi: 10.1186/s12885-015-1035-1

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© Hansen et al.; licensee BioMed Central. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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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Schematic representation of copy number variations across chromosome 17. The percentiles of SNP samples with amplification or deletion among the breast tumor samples analysed on SNP 500 K are indicated in red and blue, respectively. The positions of HER2 and the smallest amplicon containing 9 full-length genes (from 37642255 to 37970066 based on Hg19) are indicated.