Variant DetailsVariant: essv10079299Internal ID | 81115 | Landmark | | Location Information | | Cytoband | 1p13.2 | Allele length | Assembly | Allele length | hg38 | 50003 | hg19 | 50003 |
| Variant Type | CNV loss | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3587269 | Supporting Variants | | Samples | NA18523 | Known Genes | AMPD1, DENND2C | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv10079299
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|