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Table 1 Both deletions, genomic positions and genes concerned based on hg19 (GRCh37)

From: Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent disease

Chromosome region

Genomic position

Length

Count of gene symbols

Gene Symbols

Xp11.22

49,823,986-49,971,921

147936

2

AKAP4, CLCN5

Xp11.22

50,070,457-52,693,963

2623507

23

BMP15, CCNB3, CENPVP1, CENPVP2, DGKK, GSPT2, MAGED1, MAGED4, MAGED4B, NUDT10, NUDT11, SHROOM4, SNORA11D, SNORA11E, SSX7, SSX8, XAxGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B

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Molecular Cytogenetics

ISSN: 1755-8166