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. 2018 Oct 11;18:964. doi: 10.1186/s12885-018-4873-9

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© The Author(s). 2018

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. 1 — DNA copy number analysis. The genome view generated from aCGH data showed detectable aberrations in the DNA extracted from FFPE primary tumour: gain of chromosomes 2 and 7, loss of the short arm of chromosome 9, and loss of chromosomes 10, 14 and X. The aCGH data also revealed amplification of the q32.1 region (chr 1) and the EGFR gene (chr 7, black arrow), together with a homozygous deletion of the CDKN2A gene (chr 9, black arrow). aCGH: array comparative genomic hybridization; chr: chromosome