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Figure 6 | BMC Medical Genetics

Figure 6

From: Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications

Figure 6

Pedigree and haplotype data of a family with a member affected with the del22q11.2 syndrome and carrying the 3 Mb deletion caused by an interchromosomal NAHR event. The NAHR event was of maternal origin and in the previous generation there is a female AHR event within LCR22-2 that did not cause a deletion. The AHR event has been arbitrarily assigned to the mother of the deleted child.

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