Variant DetailsVariant: esv3622395 Internal ID | 6662565 | Landmark | | Location Information | | Cytoband | 10p13 | Allele length | Assembly | Allele length | hg38 | 4796 | hg19 | 4796 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13697867, essv13697874, essv13697872, essv13697870, essv13697881, essv13697884, essv13697879, essv13697869, essv13697883, essv13697885, essv13697887, essv13697877, essv13697866, essv13697875, essv13697873, essv13697878, essv13697871, essv13697882, essv13697865, essv13697886, essv13697876, essv13697868, essv13697880 | Samples | HG01098, HG02215, HG03009, NA12813, HG00138, HG00158, NA12005, HG00120, HG02490, HG01519, NA20812, HG02736, HG00232, HG03624, HG04062, HG01789, HG00708, HG01094, NA06985, HG01589, HG02651, HG00116, NA07056 | Known Genes | CCDC3 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3622395
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
|
|