Variant DetailsVariant: nsv1044136 Internal ID | 18786667 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 104933 | hg19 | 137471 | hg18 | 137471 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv749n100 | Supporting Variants | nssv3512226, nssv3504012, nssv3503001, nssv3514772, nssv3514431, nssv3707879, nssv3517074, nssv3513918, nssv3513930, nssv3518423, nssv3520209, nssv3707882, nssv3506160, nssv3507766, nssv3515099, nssv3506802, nssv3707880, nssv3507321, nssv3514614, nssv3707883, nssv3503761, nssv3707888, nssv3522027, nssv3707887, nssv3504216, nssv3504778, nssv3707884, nssv3504987, nssv3508093, nssv3504962, nssv3707881, nssv3517190, nssv3522039, nssv3707886, nssv3503445, nssv3521909, nssv3519546, nssv3506277, nssv3707885, nssv3520709, nssv3514804 | Samples | | Known Genes | FAM35BP, GPRIN2, 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) | nsv1044136
| Frequency | Sample Size | 29084 | Observed Gain | 34 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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