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

Table 1 Summary of the results from the CNV analysis

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

ISSN: 1755-8794