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. 2015 Feb 26;15:85. doi: 10.1186/s12885-015-1077-4

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© Lee 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/4.0), 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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Genomic profiles of somatic copy number alterations (SCNA). (a) Common segments (green) and Shared segments (grey). (b, c, d) Cluster P1 samples, RO1, RF, and LO4. (e, f) Cluster M samples, OM1, and OM2. (g) Cluster P2 sample, LO3. Overall the pattern of SCNA in cluster M was similar to the pattern in cluster P1 except for a large deletion on chromosome X. Cluster P2 showed distinct SCNA patterns compared to other clusters. red: amplification, blue: deletion.