1. A Genome-wide Study Reveals Copy Number Variants Exclusive to Childhood Obesity Cases 
Joseph T. Glessner, Jonathan P. Bradfield, Kai Wang, Nagahide Takahashi, Haitao Zhang, Patrick M. Sleiman, Frank D. Mentch, Cecilia E. Kim, Cuiping Hou, Kelly A. Thomas, Maria L. Garris, Sandra Deliard, Edward C. Frackelton, F. George Otieno, Jianhua Zhao, Rosetta M. Chiavacci, Mingyao Li, Joseph D. Buxbaum, Robert I. Berkowitz, Hakon Hakonarson, Struan F.A. Grant 
The American Journal of Human Genetics 
Volume 87, Issue 5, Pages (November 2010)
DOI: /j.ajhg
Copyright © 2010 The American Society of Human Genetics Terms and Conditions

2. Figure 1
Visualization of Representative Loci Most Frequently Harboring Deletions
Deletions identified at the EDIL3, S1PR5 and FOXP2 loci. Vertical blue lines indicate the SNP probe coverage. Red rectangles delineate regions of copy number variation in individual cases for deletions. RefSeq gene boundaries are shown with vertical lines delineating exons. Database of Genomic Variants entries from other studies on a variety of platforms are shown as an additional control.
The American Journal of Human Genetics  , DOI: ( /j.ajhg )
Copyright © 2010 The American Society of Human Genetics Terms and Conditions

3. Figure 2
Visualization of Representative Loci Most Frequently Harboring Duplications
Duplications identified at the KIF2B and ARL15 loci. Vertical blue lines indicate the SNP probe coverage. Green rectangles delineate regions of copy number variation in individual cases for duplications. RefSeq gene boundaries are shown with vertical lines delineating exons. Database of Genomic Variants entries from other studies on a variety of platforms are shown as an additional control.
The American Journal of Human Genetics  , DOI: ( /j.ajhg )
Copyright © 2010 The American Society of Human Genetics Terms and Conditions