Variant DetailsVariant: esv2745409 Internal ID | 9979693 | Landmark | | Location Information | | Cytoband | 12p13.33 | Allele length | Assembly | Allele length | hg38 | 612 | hg19 | 612 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6845917, essv6775659, essv6795988, essv6709452, essv6673095, essv6920119, essv6938618, essv6898855, essv6965715, essv6823585, essv6686976, essv6873637, essv6695504, essv6953181, essv6783530, essv6927893, essv6815430, essv6791813, essv6970758 | Samples | SSM071, SSM027, SSM079, SSM041, SSM028, SSM017, SSM019, SSM003, SSM031, SSM066, SSM085, SSM068, SSM005, SSM037, SSM077, SSM091, SSM070, SSM025, SSM012 | Known Genes | CACNA1C | 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) | esv2745409
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 19 | Observed Complex | 0 | Frequency | n/a |
|
|