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Fig. 2 | Molecular Cytogenetics

Fig. 2

From: Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving DOCK8, KANK1, EHMT1 genes identified by using high-resolution oligonucleotide-single nucleotide polymorphism array analysis

Fig. 2

The distribution of deletions in cases with involvement of the DOCK8 and KANK1 genes. The copy number variants in the database of genomic variation were compared to the profile of small deletions in our cohort. Segmental duplications were not flanking the deletions of the DOCK8 and KANK1 genes, which potentially excluded the pathogenic mechanism through non-homologous recombination of segmental duplications

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Molecular Cytogenetics

ISSN: 1755-8166