Fig. 10From: Clinical significance and mechanisms associated with segmental UPDAnalysis of prenatal deletion in case 9. A Case 9 showing a deletion of 10q present in all cells from a CVS chromosome analysis (top panel, arrow) that was confirmed by a region-specific FISH probe (bottom panel, arrow). B Post-delivery blood CMA revealing a copy neutral terminal ROH on chromosome 10 initiating at band q26.13 (bracket). Confirmation of segUPD is shown in Additional file 1: Figure S3Back to article page