Internal ID | 6631569 |
Landmark | |
Location Information | |
Cytoband | 2p13.1 |
Allele length | Assembly | Allele length | hg38 | 72892 | hg19 | 72892 |
|
Variant Type | CNV gain |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | essv10542472, essv10542474, essv10542473 |
Samples | HG03908, HG03391, HG03469 |
Known Genes | SEMA4F |
Method | Sequencing |
Analysis | |
Platform | Multiple platforms |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_3 |
Pubmed ID | 21293372 |
Accession Number(s) | esv3591285
|
Frequency | Sample Size | 2504 | Observed Gain | 3 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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