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. 2023 Mar 9;15:40. doi: 10.1186/s13148-023-01456-2

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© The Author(s) 2023

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/. 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 in a credit line to the data.

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Fig. 1 — Cohort overview. A. Distribution of tumour types after histopathological and molecular re-evaluation of 71 supratentorial CNS-PNETs; B and C. Further subdivision of the tumour types based on the histopathological re-evaluation; HGGs (n = 25) and OTHER diagnoses (n = 14) Abbreviations: HGG, high-grade glioma; AT/RT, atypical teratoid/rhabdoid tumour; CNS NB-FOXR2, CNS neuroblastoma, FOXR2-activated; ETMR, embryonal tumour with multilayered rosettes; EPN, ependymoma; DHG, H3 G34-mutant, diffuse hemispheric glioma H3 G34-mutant; DMG, K27, diffuse midline glioma H3 K27-altered; IHG, infant-type hemispheric glioma; HGG NOS, high-grade glioma not otherwise specified; PBL, pineoblastoma; CPC, choroid plexus carcinoma