Variant DetailsVariant: nsv1036598Internal ID | 18779129 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 63437 | hg19 | 63437 | hg18 | 63437 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv747n100 | Supporting Variants | nssv3514727, nssv3518669, nssv3510026, nssv3522730, nssv3507571, nssv3512569, nssv3517313, nssv3510930, nssv3509099, nssv3509464, nssv3519197, nssv3518755, nssv3507247, nssv3521673, nssv3521856, nssv3512112, nssv3507079, nssv3518097, nssv3508536, nssv3516291, nssv3517779, nssv3505842, nssv3506675 | Samples | | Known Genes | FAM35BP, SYT15 | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | nsv1036598
| Frequency | Sample Size | 29084 | Observed Gain | 10 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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