Variant DetailsVariant: esv3622726Internal ID | 6662895 | Landmark | | Location Information | | Cytoband | 10p12.1 | Allele length | Assembly | Allele length | hg38 | 1917 | hg19 | 1917 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13733569, essv13733563, essv13733573, essv13733559, essv13733560, essv13733576, essv13733575, essv13733558, essv13733578, essv13733574, essv13733566, essv13733579, essv13733570, essv13733567, essv13733562, essv13733572, essv13733561, essv13733564, essv13733568, essv13733565, essv13733577, essv13733571 | Samples | HG02072, HG00458, HG01843, HG00451, HG01849, NA18986, HG01851, HG01797, HG00557, HG02522, HG01852, HG00692, HG02048, NA18963, HG02127, HG01811, HG01874, NA18591, HG04161, HG01869, NA19063, HG00581 | Known Genes | RAB18 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3622726
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 22 | Observed Complex | 0 | Frequency | n/a |
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