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Table 1 Summary of the results from the CNV analysis

From: Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family

Chromosome Start End Size (kb) CNV Patient Genes within or close to the CNV
5q31.2 137,660,826 137,724,036 63 del 304 CDC25C, FAM53C, KDM3B
6q26 161,354,191 161,558,170 204 dup 3 MAP3K4, AGPAT4
7q11.22 71,665,416 71,714,246 49 del 1 CALN1
9q31.1 105,763,417 105,822,396 59 del 322 CYLC2
12p13.31 6,643,315 6,671,120 28 dup 830 GAPDH, IFFO1, NOP2
12q24.23 119,981,576 119,994,376 13 del 301 No genes
19p13.11 19,943,909 19,966,901 19 dup 322 No genes
19q13.42 55,622,908 55,641,955 19 dup 830 PPP1R12C