Figure 1
From: Characteristics of rare and private deletions identified in phenotypically normal individuals
Chromosomal microarray testing results. The identified deletions are shown in Gene View created by the Agilent Genomic Workbench (Agilent Technologies). (a) subject 1, (b) subject 2, (c) subject 3, (d) subject 4, and (e) subject 5. Previously reported deletions that overlapped with the deletions reported in this study are depicted by blue rectangles or pentagons for comparison. Directions suggested by the pentagons indicate large deletions beyond the edge. All genomic positions are unified to the hg19 assembly.
