Internal ID | 6676101 |
Landmark | |
Location Information | |
Cytoband | 15q13.1 |
Allele length | Assembly | Allele length | hg38 | 66457 | hg19 | 66457 |
|
Variant Type | CNV gain |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | essv15198899, essv15198900, essv15198898 |
Samples | NA18489, HG02143, HG03039 |
Known Genes | HERC2 |
Method | Sequencing |
Analysis | |
Platform | Multiple platforms |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_3 |
Pubmed ID | 21293372 |
Accession Number(s) | esv3635991
|
Frequency | Sample Size | 2504 | Observed Gain | 3 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|