List of variants reported as likely pathogenic for partial deletion of chromosome 11

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.965+1G>A	rs771527206	0.00001
NM_001368894.2(PAX6):c.256G>C (p.Gly86Arg)	rs759557055
NM_002017.5(FLI1):c.1010G>A (p.Arg337Gln)	rs1064797086
NM_024426.6(WT1):c.1016+1G>A	rs2133032244
NM_024426.6(WT1):c.1016+2T>G	rs1852674417
NM_024426.6(WT1):c.1114-1G>T	rs1851976798
NM_024426.6(WT1):c.1297T>G (p.Cys433Gly)	rs121907905
NM_024426.6(WT1):c.1406A>G (p.Asp469Gly)	rs121907902
NM_024426.6(WT1):c.1498C>T (p.Arg500Trp)
NM_024426.6(WT1):c.512G>T (p.Gly171Val)	rs1554946480
NM_024426.6(WT1):c.888-2A>G
NM_024426.6(WT1):c.965+2T>C
Single allele

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