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. 2020 Jun 19;10(6):70. doi: 10.1038/s41408-020-0336-z

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© The Author(s) 2020

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. 1 — a pPCL is enriched for adverse risk copy number alterations compared to MM¹⁷, *p < 0.05. Significant genes are labeled, with the exception of markers on chromosomes associated with hyperdiploidy. b The frequency of driver mutations in pPCL and MM, *p < 0.05 (chi-square test); ⁺p < 0.005 (after multiple test correction).