From: Evaluation of the X-Linked High-Grade Myopia Locus (MYP1) with Cone Dysfunction and Color Vision Deficiencies Invest. Ophthalmol. Vis. Sci.. 2009;50(4):1552-1558.

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From: Evaluation of the X-Linked High-Grade Myopia Locus (MYP1) with Cone Dysfunction and Color Vision Deficiencies Invest. Ophthalmol. Vis. Sci.. 2009;50(4):1552-1558. doi:10.1167/iovs.08-2455 Figure Legend: Fine-tiling array-CGH analysis screening for copy number variations on the MYP1 (Xq28) locus in the BED and Minnesota pedigrees. Both pedigrees showed predicted duplications of the opsin gene array (approximately at 153 megabases), whereas the Minnesota pedigree showed an additional intergenic deletion and an intergenic duplication (approximately at 154 megabases). Array-CGH y-axis represents log2 ratio (calculated by subtracting the log value of the reference sample intensity from the log of the test sample intensity); y ≥ 0.25 is considered a variation. Average probe spacing was 340 bp. Data were uploaded as custom tracks on to the University of California at Santa Cruz genome browser (http://genome.uscs.edu/) for visualization and comparison. Date of download: 10/31/2017 The Association for Research in Vision and Ophthalmology Copyright © 2017. All rights reserved.