Variant DetailsVariant: esv3595035Internal ID | 6635310 | Landmark | | Location Information | | Cytoband | 3p26.3 | Allele length | Assembly | Allele length | hg38 | 1291 | hg19 | 1291 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv10899619, essv10899621, essv10899622, essv10899618, essv10899620, essv10899617 | Samples | NA19819, NA19471, NA19451, NA19030, HG02805, NA19429 | Known Genes | CNTN4 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3595035
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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