Internal ID | 6656356 |
Landmark | |
Location Information | |
Cytoband | 8p23.1 |
Allele length | Assembly | Allele length | hg38 | 1708 | hg19 | 1708 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | essv13093744, essv13093743 |
Samples | NA20761, HG01684 |
Known Genes | |
Method | Sequencing |
Analysis | |
Platform | Multiple platforms |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_3 |
Pubmed ID | 21293372 |
Accession Number(s) | esv3616159
|
Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
|