Variant DetailsVariant: esv3633240Internal ID | 6673362 | Landmark | | Location Information | | Cytoband | 13q32.1 | Allele length | Assembly | Allele length | hg38 | 656 | hg19 | 656 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14868841, essv14868844, essv14868843, essv14868845, essv14868848, essv14868847, essv14868849, essv14868838, essv14868834, essv14868835, essv14868839, essv14868840, essv14868837, essv14868846, essv14868842, essv14868836, essv14868833 | Samples | NA19028, HG02628, HG02973, HG02419, HG03295, NA20356, HG03082, HG02461, NA19385, NA19026, HG02009, HG03061, HG03109, HG01894, NA19144, NA19310, HG03066 | Known Genes | ABCC4 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3633240
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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