Internal ID | 6662612 |
Landmark | |
Location Information | |
Cytoband | 10p13 |
Allele length | Assembly | Allele length | hg38 | 119156 | hg19 | 119156 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | essv13704096 |
Samples | HG01796 |
Known Genes | FAM171A1 |
Method | Sequencing |
Analysis | |
Platform | Multiple platforms |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_3 |
Pubmed ID | 21293372 |
Accession Number(s) | esv3622442
|
Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|