|
Status |
Public on Nov 30, 2015 |
Title |
Rare CNVs in Lynch Syndrome patients negative for mutations in mismatch repair genes |
Organism |
Homo sapiens |
Experiment type |
Genome variation profiling by genome tiling array Genome variation profiling by SNP array
|
Summary |
This SuperSeries is composed of the SubSeries listed below.
|
|
|
Overall design |
Refer to individual Series
|
|
|
Citation missing |
Has this study been published? Please login to update or notify GEO. |
Submission date |
Sep 02, 2015 |
Last update date |
Jul 13, 2018 |
Contact name |
Rolando Andre Rios Villacis |
E-mail(s) |
rolando.andre@unb.br
|
Phone |
+5561996912223
|
Organization name |
University of BrasÃlia - UnB
|
Department |
Genetics and Morphology
|
Lab |
Genetic Toxicology
|
Street address |
Asa Norte
|
City |
BrasÃlia |
State/province |
DF |
ZIP/Postal code |
70910-900 |
Country |
Brazil |
|
|
Platforms (2) |
GPL10150 |
Agilent-022060 SurePrint G3 Human CGH Microarray 4x180K (Probe Name version) |
GPL16131 |
[CytoScanHD_Array] Affymetrix CytoScan HD Array |
|
Samples (67)
|
|
This SuperSeries is composed of the following SubSeries: |
GSE72665 |
Rare CNVs in Lynch Syndrome patients negative for mutations in mismatch repair genes [Agilent] |
GSE72667 |
Rare CNVs in Lynch Syndrome patients negative for mutations in mismatch repair genes [Affymetrix] |
|
Relations |
BioProject |
PRJNA294618 |