|
| Status |
Public on Jan 23, 2015 |
| Title |
SMC2: a candidate gene associated with Cornelia de Lange Syndrome |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by genome tiling array
|
| Summary |
whole-genome aCGH analysis also showed us that the patient carried a 12.01-1M Mb deletion region at chromosome bands 9q31.1-q32 (105,190,105-117,195,154). The deleted region encompasses 22 genes including SMC2
|
| |
|
| Overall design |
Two-condition Samples, Cornelia de Lange Syndrome vs. Normal cells.
|
| |
|
| Contributor(s) |
Cao R, Long F, Fang S, Xu Y, Xu R, Chen S |
| Citation missing |
Has this study been published? Please login to update or notify GEO. |
| Submission date |
Jan 23, 2014 |
| Last update date |
Oct 27, 2015 |
| Contact name |
wang liang |
| E-mail(s) |
wangliangkexue@163.com
|
| Organization name |
BioChainBJ
|
| Street address |
7A North Yongchang Road BDA
|
| City |
Beijing |
| ZIP/Postal code |
100176 |
| Country |
China |
| |
|
| Platforms (1) |
| GPL10150 |
Agilent-022060 SurePrint G3 Human CGH Microarray 4x180K (Probe Name version) |
|
| Samples (1) |
| GSM1313634 |
Cornelia de Lange Syndrome aCGH expriment |
|
| Relations |
| BioProject |
PRJNA236306 |
