Variant DetailsVariant: esv3603917| Internal ID | 6990948 | | Landmark | | | Location Information | | | Cytoband | 5p15.31 | | Allele length | | Assembly | Allele length | | hg38 | 3650 | | hg19 | 3650 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv11802092, essv11802093, essv11802096, essv11802098, essv11802100, essv11802094, essv11802091, essv11802095, essv11802097, essv11802099 | | Samples | HG00304, HG00177, HG01503, HG01766, NA07048, HG03911, NA12760, HG01791, HG00240, HG02790 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3603917
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 10 | | Observed Complex | 0 | | Frequency | n/a |
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