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Figure 1 | Molecular Cytogenetics

Figure 1

From: Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders

Figure 1

Results of array-CGH analysis in our cases 1, 2, 3, and 4. A) Array-CGH analysis in patient 1 shows ~ 269 kb deletion at 7q31.1 (chr7:110,879,586-111,149,166) including exon 3 of IMMP2L gene. B) Array-CGH analysis in patient 2 shows a ~ 152.7 kb deletion at 7q31.1 (chr7:111,066,736-111,201,968). The deletion encompasses exons 1, 2, and 3 of IMMP2L gene. C) Array-CGH analysis in patient 3 shows the presence of ~249.9 kb deletion at 7q31.1 (chr7:111,066,736-111,316,651) encompassing exons 1, 2, and 3 of IMMP2L gene. D) Array-CGH analysis in patient 4 shows a ~307.7 kb duplication at 7q31.1 (chr7:110,135,083-110,505,806) including exon 6 of IMMP2L gene. E) Schematic representation of deleted regions in patients 1, 2, and 3 and of duplicated region in patient 4.

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Molecular Cytogenetics

ISSN: 1755-8166