Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain (original) (raw)
Figure 2
Overview of the delineated regulatory and FOXL2 encompassing deletions.
Overview of the FOXL2 region (chr3:135099979–142458004; UCSC, Human Genome Browser, hg19) with custom tracks showing the delineated regulatory and FOXL2 encompassing deletions presented in this study, numbered from A to H and from 1 to 16 respectively. The horizontal red bars indicate the deleted regions (regulatory deletions are shown in dark red and FOXL2 encompassing deletions are shown in light red). At the top, the RefSeq Genes track is included. The locations of FOXL2 and long non-coding RNA PISRT1 are indicated by vertical blue and yellow lines respectively. Additional information on genes (i) contained in the deletion, (ii) spanning the breakpoints, or (iii) located outside the respective deletion and their distances to the breakpoint, can be found in Table S1.