Variant DetailsVariant: esv3637825 | Internal ID | 7024613 | | Landmark | | | Location Information | | | Cytoband | 16p13.2 | | Allele length | | Assembly | Allele length | | hg38 | 2015 | | hg19 | 2015 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv15368190, essv15368200, essv15368197, essv15368231, essv15368199, essv15368196, essv15368207, essv15368198, essv15368204, essv15368191, essv15368194, essv15368233, essv15368215, essv15368201, essv15368222, essv15368195, essv15368216, essv15368234, essv15368238, essv15368203, essv15368211, essv15368192, essv15368218, essv15368225, essv15368206, essv15368214, essv15368230, essv15368210, essv15368212, essv15368224, essv15368237, essv15368202, essv15368209, essv15368232, essv15368239, essv15368217, essv15368227, essv15368236, essv15368221, essv15368213, essv15368219, essv15368223, essv15368208, essv15368193, essv15368226, essv15368228, essv15368235, essv15368229, essv15368220, essv15368205 | | Samples | NA21110, HG04096, NA18639, HG02691, HG03926, HG03963, NA12400, HG03944, HG03680, HG04156, HG01522, HG03009, NA21108, HG02603, HG03762, HG01080, HG03693, HG00323, HG03902, HG03697, HG03908, HG03861, HG01200, HG01595, HG03644, NA20505, NA21119, HG00368, HG00583, HG00275, NA18579, HG03967, HG01073, HG03740, HG01075, HG03653, NA21113, NA20773, HG00625, NA20804, NA07051, NA20530, NA20778, HG03681, HG01395, HG03789, NA18552, HG01061, HG00362, HG03741 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3637825
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 50 | | Observed Complex | 0 | | Frequency | n/a |
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