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. Author manuscript; available in PMC: 2024 Aug 6.
Published in final edited form as: Mutat Res. 2021 Dec 14;824:111773. doi: 10.1016/j.mrfmmm.2021.111773

Fig. 1. Distribution of chromosomal aberration endpoints in human cancers.

Fig. 1.

A. Diagrams showing some of the possible intra- and inter-chromosomal aberrations. An aberration is defined as improper connection of two breakpoints (1st and 2nd). This can result in intra-chromosomal deletion, inversion or duplication and various inter-chromosomal duplications. B. Frequency of intra- and inter-chromosomal aberrations. “Other” represents complex or not specified forms of aberrations. C. Genome density of the two aberration endpoints (breakpoints) leading to the aberrations in A. The approximate chromosome location is indicated on top. D, E. Size of intrachromosomal deletions (D) or other intra-chromosomal aberrations (E) in base pairs.