Variant DetailsVariant: dgv802e201Internal ID | 20125689 | Landmark | | Location Information | | Cytoband | 4p16.3 | Allele length | Assembly | Allele length | hg38 | 1319 | hg19 | 1319 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2726759, esv2726757, esv2726755 | Samples | SSM083, SSM027, SSM065, SSM097, SSM013, SSM050, SSM002, SSM028, SSM084, SSM017, SSM019, SSM032, SSM067, SSM086, SSM033, SSM066, SSM068, SSM016, SSM077, SSM022, SSM055, SSM025, SSM012 | Known Genes | RNF212 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | dgv802e201
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
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