Internal ID | 6639406 |
Landmark | |
Location Information | |
Cytoband | 3q28 |
Allele length | Assembly | Allele length | hg38 | 51877 | hg19 | 51877 |
|
Variant Type | CNV gain |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | essv11273230 |
Samples | HG00704 |
Known Genes | FGF12 |
Method | Sequencing |
Analysis | |
Platform | Multiple platforms |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_3 |
Pubmed ID | 21293372 |
Accession Number(s) | esv3599140
|
Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|