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. 2020 Oct 16;216(4):905–930. doi: 10.1534/genetics.120.303596

Figure 3.

Figure 3

Complex sex chromosome aneuploidy and mosaicism in an F1 male. (A) The panel shows the chromosomal sex and mitochondria complement of the parents and F1 individual. Blue denotes C57BL/6J and red denotes 129X1/SvJ. (B) This panel is a reprint of Figure 1 and was used to classify the F1 male, shown as a yellow circle, as an XXY based on the x- and y-axis intensities (two X chromosomes and a Y chromosome present). This panel also provides evidence of mosaicism for the presence and absence of the Y chromosome (based on the low Y chromosome intensity). (C) This panel provides evidence of mosaicism for the X chromosome and identifies the paternal origin (129X1/SvJ) of the chromosome lost in some cells. The plot presents the intensities of the two alternate alleles for 173 X chromosome markers that are informative between the two parents. Four individuals are shown: a C57BL/6J female in blue, a 129X1/SvJ male in red, a (C57BL/6Jx129X1/SvJ)F1 female in gray, and the F1 male case in yellow. The shapes denote the type of call made by the Illumina software: circles are homozygous A, T, C, or G calls; triangles are H calls; and squares are N calls. (D) This panel shows the proposed sex chromosome complement of the two types of cells present in this F1 male case. This solution explains the observations from previous three panels.