Variant DetailsVariant: esv3586345Internal ID | 6626658 | Landmark | | Location Information | | Cytoband | 1p31.1 | Allele length | Assembly | Allele length | hg38 | 15232 | hg19 | 15232 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv9963917, essv9963915, essv9963916, essv9963913, essv9963914 | Samples | NA18561, HG02836, HG03246, HG01871, HG00690 | Known Genes | LRRC7, PIN1P1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3586345
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 5 | Observed Complex | 0 | Frequency | n/a |
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