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Figure 2 | BMC Medical Genetics

Figure 2

From: Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder

Figure 2

Adapted screenshot from the UCSC genome browser [36]showing the rearranged 6q-region. The FISH-probes used to characterize the rearrangements are shown in red. The figure shows a gap region of unmapped sequence, which also is the likely point for the translocation breakpoint on chromosome 6. A large (~400kbp) deletion is found telomeric of the translocation and encompasses the GPR63, NDUFA4 and KLHL32 genes. An overlapping deletion found in another study [32] is also displayed.

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