Skip to main content
Fig. 2 | Italian Journal of Pediatrics

Fig. 2

From: Incidental finding of APC deletion in a child: double trouble or double chance? – a case report

Fig. 2

Pathogenic CNVs of the patient. a It is shown part of array-CGH results of the patient, focusing on the 2.5 Mb deletion on the long arm of chromosome 22 at band q11.21 that involve 43 OMIM genes. b It is represented the 3.6 Mb deletion on the long arm of chromosome 5 at band q21.3q22.2 that involve 12 OMIM genes, including APC. The breakpoints are reported according to the 37 build (March 2009) of the Human Genome Reference consortium (GRch37/hg19)

Back to article page
\