Internal ID | 3705911 |
Landmark | |
Location Information | |
Cytoband | 10p13 |
Allele length | Assembly | Allele length | hg38 | 2252 | hg19 | 2252 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | Heterozygous |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | esv3622441 |
Supporting Variants | |
Samples | NA19658 |
Known Genes | FAM171A1 |
Method | Sequencing |
Analysis | |
Platform | Multiple platforms |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_3 |
Pubmed ID | 21293372 |
Accession Number(s) | essv13704095
|
Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|