|
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 |