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. 2015 Aug 19;16:61. doi: 10.1186/s12881-015-0213-y

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© van Minkelen et al. 2015

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 1 — Results SNP array analysis. Indicated in the figure are the zygosity (heterozygous: yellow bars; homozygous: red bars) and Log2Ratio (reds square: deleted region based on Log2Ratio) tracks, the locations of APTX and surrounding genes on chromosome 9p21.1 (NCBI 37; UCSC hg19), and the exon numbering of APTX for our index patient (a) and the reference sample of Dr. Yoon et al. (b)