Variant DetailsVariant: essv13992145Internal ID | 3993961 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg38 | 178751 | hg19 | 178751 |
| Variant Type | CNV gain | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3625083 | Supporting Variants | | Samples | HG03830 | Known Genes | AP2A2, CHID1, MUC6, TSPAN4 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv13992145
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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