Internal ID | 15187978 |
Landmark | |
Location Information | |
Cytoband | 14q22.3 |
Allele length | Assembly | Allele length | hg38 | 11220 | hg19 | 11220 | hg18 | 11220 | hg17 | 11220 |
|
Variant Type | CNV deletion |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | nsv1289 |
Supporting Variants | |
Samples | NA12156 |
Known Genes | SLC35F4 |
Method | Sequencing |
Analysis | End-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005) |
Platform | Capillary |
Comments | |
Reference | Kidd_et_al_2008 |
Pubmed ID | 18451855 |
Accession Number(s) | nssv9200
|
Frequency | Sample Size | 9 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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