Internal ID | 15503865 |
Landmark | |
Location Information | |
Cytoband | 1p36.21 |
Allele length | Assembly | Allele length | hg38 | 12536 | hg19 | 12536 | hg18 | 12536 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | nssv626032 |
Samples | 1 |
Known Genes | FLJ37453 |
Method | SNP array |
Analysis | Analysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array |
Platform | GPL8882 |
Comments | |
Reference | Arlt_et_al_2011 |
Pubmed ID | 21212237 |
Accession Number(s) | nsv511126
|
Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|