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. 2021 Jul 6;480(2):481–486. doi: 10.1007/s00428-021-03140-3

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — IGV split-screen view of read alignments of the identified CREM-EWSR1 (Case 1) and CREM-FUS (Case 2) fusion events. Shown are the breakpoints in the CREM (left) and the EWSR1/FUS (right) genes, respectively. Alignments whose mate pairs are mapped to the fusion sequence on the other chromosome are colored in dark green/pink for CREM-EWSR1 and ocher/pink for CREM-FUS. All other alignments are colored gray