Variant DetailsVariant: essv10079208Internal ID | 81024 | Landmark | | Location Information | | Cytoband | 1p13.2 | Allele length | Assembly | Allele length | hg38 | 355811 | hg19 | 355811 |
| Variant Type | CNV loss | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3587239 | Supporting Variants | | Samples | NA18523 | Known Genes | AP4B1-AS1, MAGI3, PHTF1, PTPN22, RSBN1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv10079208
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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