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Figure 1 | Journal of Medical Case Reports

Figure 1

From: Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report

Figure 1

Array comparative genomic hybridisation scatter plot. An array comparative genomic hybridisation scatter plot for chromosome 1 generated by BlueFuse microarray analysis software (BlueGnome) showing the five Bacterial Artificial Chromosome clone deletions (BACs RP3-395M20, RP11-333E3, RP4-785P20, RP11-46F15 and RP1-286D) within 1p36.32 (arrowed) and the two Bacterial Artificial Chromosome clone duplications (BACs RP11-117D22 and RP11-243A18) within 1p32.3 (asterisked). The log2 ratios of the patient vs. reference DNA is shown on the vertical axis (mean log2 ratio of -0.6 for the deletion and 0.38 for the amplification) and the position of each Bacterial Artificial Chromosome along chromosome 1 is shown along the horizontal line. The location of the observed abnormalities is viewed in relation to a chromosome 1 ideogram, with the deletion represented in red and the duplication represented in green.

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Journal of Medical Case Reports

ISSN: 1752-1947