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. 2019 Nov 29;9(12):96. doi: 10.1038/s41408-019-0257-x

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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. 3 — a At least one clonal DH-JH or VH(DH)JH rearrangement was identified in 172/183 cases indicative of an IGH germline status in the remaining 11 cases. b A FOXI3-JH6 genomic fusion breakpoint was identified in case ALL UPN22. Fifty eight breakpoint spanning reads covered the breakpoint and for the same sample VIDJIL identified two different clonal rearrangements with 66 and 72 reads, respectively. c For UPN30 two genomic fusion breakpoints (BCL7C-Dδ3 and Dδ2-BCL7C) were sequenced. The different breakpoints were located 11.5 Kb downstream of the BCL7C stop codon.